Gene: STEAP1B

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 7

Location in Chromosome : 7p15.3

Description of this Gene: STEAP family member 1B

Type of Gene: protein-coding

rs10155981 in STEAP1B gene and Bilirubin level result PMID 22085899 2012 UGT1A1 is a major locus influencing bilirubin levels in African Americans.

rs10155981 in STEAP1B gene and Bilirubin measurement PMID 22085899 2012 UGT1A1 is a major locus influencing bilirubin levels in African Americans.

rs59084784 in STEAP1B gene and Birth Weight PMID 31043758 2019 Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.

rs1880241 in STEAP1B gene and Body Height PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs1880241 in STEAP1B gene and C-reactive protein measurement PMID 30388399 2018 Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.

PMID 21196492 2011 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus.

PMID 29403010 2018 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

rs1548418 in STEAP1B gene and Esophageal Neoplasms PMID 22960999 2012 Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.

rs76659285 in STEAP1B gene and Finding of Mean Corpuscular Hemoglobin PMID 29403010 2018 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

rs13242809 in STEAP1B gene and Lymphocyte Count measurement PMID 27863252 2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

rs74702905 in STEAP1B gene and Serum albumin measurement PMID 29403010 2018 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.